![]() Just as the energy required to excite an electron in a particular atom is fixed, the energy required to change the vibration of a particular chemical bond is also fixed. This type of radiation is usually not energetic enough to excite electrons, but it will cause the chemical bonds within molecules to vibrate in different ways. However, lower energy radiation in the infrared (IR) region of the spectrum can also produce changes within atoms and molecules. Because the flame’s temperature is greatest at its center, the concentration of analyte atoms in an excited state is greater at the flame’s center than at its outer edges.So far, we have been talking about electronic transitions, which occur when photons in the UV-visible range of the spectrum are absorbed by atoms. An additional chemical interference results from self-absorption. Instruments may contain as many as 48–60 detectors.įlame emission is subject to the same types of chemical interferences as atomic absorption they are minimized using the same methods: by adjusting the flame’s composition and by adding protecting agents, releasing agents, or ionization suppressors. Schematic diagram of a multichannel atomic emission spectrometer for the simultaneous analysis of several elements. , couples a monochromator with multiple detectors that are positioned in a semicircular array around the monochromator at positions that correspond to the wavelengths for the analytes. A simple design for a multichannel spectrometer, shown in Figure 10.7.3 This sequential analysis allows for a sampling rate of 3–4 analytes per minute.Īnother approach to a multielemental analysis is to use a multichannel instrument that allows us to monitor simultaneously many analytes. If the instrument includes a scanning monochromator, we can program it to move rapidly to an analyte’s desired wavelength, pause to record its emission intensity, and then move to the next analyte’s wavelength. Schematic diagram of an inductively coupled plasma torch.Ītomic emission spectroscopy is ideally suited for a multielemental analysis because all analytes in a sample are excited simultaneously. This is accomplished by the tangential flow of argon shown in the schematic diagram. At these high temperatures the outer quartz tube must be thermally isolated from the plasma. The resulting collisions with the abundant unionized gas give rise to resistive heating, providing temperatures as high as 10000 K at the base of the plasma, and between 60 K at a height of 15–20 mm above the coil, where emission usually is measured. An alternating radio-frequency current in the induction coil creates a fluctuating magnetic field that induces the argon ions and the electrons to move in a circular path. Plasma formation is initiated by a spark from a Tesla coil. The sample is mixed with a stream of Ar using a nebulizer, and is carried to the plasma through the torch’s central capillary tube. The ICP torch consists of three concentric quartz tubes, surrounded at the top by a radio-frequency induction coil. Because a plasma operates at a much higher temperature than a flame, it provides for a better atomization efficiency and a higher population of excited states.Ī schematic diagram of the inductively coupled plasma source (ICP) is shown in Figure 10.7.2 A plasma’s high temperature results from resistive heating as the electrons and argon ions move through the gas. The plasma used in atomic emission is formed by ionizing a flowing stream of argon gas, producing argon ions and electrons. We also expect emission intensity to increase with temperature.Ī plasma is a hot, partially ionized gas that contains an abundant concentration of cations and electrons. ![]() ![]() We expect that excited states with lower energies have larger populations and more intense emission lines. ![]()
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